The FAM20C gene homepage

General information
Gene symbol FAM20C
Gene name family with sequence similarity 20, member C
Chromosome 7
Chromosomal band p22.3
Imprinted Unknown
Genomic reference NG_033970.1
Transcript reference NM_020223.3
Exon/intron information NM_020223.3 exon/intron table
Associated with diseases ID, RNS
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 56
Unique public DNA variants reported 46
Individuals with public variants 43
Hidden variants 15
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated February 26, 2024
Version FAM20C:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_020223.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/FAM20C
HGNC 22140
Entrez Gene 56975
PubMed articles FAM20C
OMIM - Gene 611061
OMIM - Diseases RNS (Raine syndrome (RNS))
HGMD FAM20C
GeneCards FAM20C
GeneTests FAM20C
Orphanet FAM20C


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00007401 7 family with sequence similarity 20, member C NM_020223.3 NP_064608.2 56


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